Clinical, microbiologic, and genetic determinants of persistent methicillin-resistant Staphylococcus aureus bacteremia

被引:56
|
作者
Neuner, Elizabeth A. [1 ]
Casabar, Ed [2 ]
Reichley, Richard [3 ]
McKinnon, Peggy S. [4 ]
机构
[1] Cleveland Clin, Dept Pharm, Cleveland, OH 44195 USA
[2] Barnes Jewish Hosp, Dept Pharm, St Louis, MO 63310 USA
[3] BJC Healthcare, Dept Med Informat, St Louis, MO 63310 USA
[4] Cubist Pharmaceut, Lexington, MA 02421 USA
关键词
MRSA; Vancomycin; Bacteremia; VANCOMYCIN THERAPY; RISK-FACTORS; SCCMEC TYPE; INFECTIONS; DEFINITIONS; PREDICTORS; PNEUMONIA; EFFICACY; OUTCOMES; FAILURE;
D O I
10.1016/j.diagmicrobio.2010.02.026
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Methicillin-resistant Staphylococcus aureus bacteremia (MRSAB) often persists despite full susceptibility to vancomycin; therefore, associated factors were assessed. A retrospective cohort analysis of 222 patients with MRSAB treated with vancomycin was conducted; patients with persistent MRSAB (pMRSAB) were compared to those with nonpersistent bacteremia (NPB). Incidence of pMRSAB was 9%. More patients with vancomycin MIC = 2 mg/L had pMRSAB (16%) compared to patients with vancomycin MIC <2 mg/L (5%), P = 0.012. SCCmec type and Panton-Valentine leukocidin production were similar between patients with pMRSAB and NPB. There was no difference in vancomycin troughs, time to first dose, or area under the concentration-time curve/MIC between groups. More metastatic complications were observed in pMRSAB 63% versus NPB 32% (P = 0.005). Multivariate analysis found endocarditis (odds ratio [OR], 2.3; P = 0.021), complicated MRSAB (OR, 2.6; P = 0.009), vancomycin MIC = 2 (OR, 2.6; P = 0.009), and septic shock (OR 2.2 P = 0.031), which were independent predictors of pMRSAB. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:228 / 233
页数:6
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